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Author Spotlight: Unveiling the Role of TMOD3 in Platinum Resistance and Immune Infiltration in Ovarian Cancer
Published on: August 2, 2024
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Expression of human dCTP pyrophosphatase 1 (DCTPP1) and its association with cisplatin resistance characteristics in
Yu Wang1,2, Xiangyun Chen2, Qiduan Chen1
1Obstetrics and Gynecology center, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Journal of Cellular and Molecular Medicine
|April 30, 2024
Summary
dCTP pyrophosphatase 1 (DCTPP1) is overexpressed in ovarian cancer, contributing to cisplatin resistance. Targeting DCTPP1 may overcome this resistance by enhancing oxidative stress and reactive oxygen species accumulation.
Area of Science:
- Oncology
- Biochemistry
- Molecular Biology
Background:
- Cisplatin resistance significantly challenges ovarian cancer treatment.
- dCTP pyrophosphatase 1 (DCTPP1) is a newly identified enzyme influencing cancer traits and drug responses.
Purpose of the Study:
- To investigate the role of DCTPP1 in ovarian cancer progression.
- To determine DCTPP1's impact on cisplatin response and resistance.
Main Methods:
- Bioinformatic analysis of publicly available ovarian cancer databases.
- Analysis of DCTPP1 expression in cisplatin-sensitive and resistant cell lines (SKOV3/S, SKOV3/DDP) and patient samples.
- Investigation of DCTPP1's effect on reactive oxygen species (ROS) and oxidative stress.
Main Results:
- DCTPP1 is significantly overexpressed in ovarian cancer, correlating with tumor progression and poor prognosis post-cisplatin treatment.
- DCTPP1 is linked to cisplatin resistance pathways, including pyrimidine metabolism and P53 signaling.
- Higher DCTPP1 expression observed in resistant cells/samples; its knockout reversed cisplatin resistance by increasing ROS and antioxidant response.
Conclusions:
- DCTPP1 is a potential prognostic biomarker for ovarian cancer patients.
- Targeting DCTPP1 presents a promising strategy to overcome cisplatin resistance in ovarian cancer therapy.

